Canonical Allele Identifier: CA1129841065

Gene: RXRA

Linked Data

• dbSNP Id: rs1831088615
• gnomAD v3: 9-134408200-CT-C
• gnomAD v4: 9-134408200-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.134408201del , CM000671.2:g.134408201del	GRCh38
NC_000009.11:g.137300047del , CM000671.1:g.137300047del	GRCh37
NC_000009.10:g.136439868del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481739.2:c.332del MANE Select	ENSP00000419692.1:p.Leu111ArgfsTer?
ENST00000672570.1:c.251del	ENSP00000500402.1:p.Leu84ArgfsTer?
ENST00000356384.4:n.742del
ENST00000481739.1:c.332del	ENSP00000419692.1:p.Leu111ArgfsTer?
NM_001291920.1:c.251del	NP_001278849.1:p.Leu84ArgfsTer?
NM_001291921.1:c.41del	NP_001278850.1:p.Leu14ArgfsTer?
NM_002957.5:c.332del	NP_002948.1:p.Leu111ArgfsTer?
NM_002957.6:c.332del MANE Select	NP_002948.1:p.Leu111ArgfsTer?
NM_001291921.2:c.41del	NP_001278850.1:p.Leu14ArgfsTer?
NM_001291920.2:c.251del	NP_001278849.1:p.Leu84ArgfsTer?